AU2002222682B8 - Tropolone Derivatives - Google Patents
Tropolone Derivatives Download PDFInfo
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- AU2002222682B8 AU2002222682B8 AU2002222682A AU2002222682A AU2002222682B8 AU 2002222682 B8 AU2002222682 B8 AU 2002222682B8 AU 2002222682 A AU2002222682 A AU 2002222682A AU 2002222682 A AU2002222682 A AU 2002222682A AU 2002222682 B8 AU2002222682 B8 AU 2002222682B8
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- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/74—Naphthothiophenes
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- C07C233/30—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
- C07C233/33—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
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- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/266—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of hydrocarbons and halogenated hydrocarbons
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- C07C225/20—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the carbon skeleton
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- C07C225/22—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07C233/30—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
- C07C233/32—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
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- C07C233/76—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by doubly-bound oxygen atoms
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- C07C245/02—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides
- C07C245/06—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings
- C07C245/10—Azo compounds, i.e. compounds having the free valencies of —N=N— groups attached to different atoms, e.g. diazohydroxides with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings with nitrogen atoms of azo groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems
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- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/38—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by doubly-bound oxygen atoms
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- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/20—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
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- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
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- C07C49/753—Unsaturated compounds containing a keto groups being part of a ring containing ether groups, groups, groups, or groups
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- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
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- Chemical & Material Sciences (AREA)
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Description
WO 02/053523 WO 02153523PCT/JPOl/11083 L 7 Junlo.eiia Ceity)98 o. 1 8 1 .12 ~Jl~'ti-.Z'-A-00-U If (EA RDMA, Siene 240,b p9,98 Strct F jucnal 6, pp.cna 11-2,191Chit, 198, etl a Bioc. B1, ph182 WO 02/053523 WO 02/53523PCT/JP01111083 Res. Commun., 166, pp. 1300-1307, 1990 MiA TW-0" 44t L- 1- ~f t-h-t 0
R
2 Ar XY
R
3
R
-Z~i RI~J RI b W .CtI<(LoM:-7D±L1iIU1 WO 02/053523 WO 02/53523PCT/JP01111083 7iJ'E~i c 9 7/-At' t U cc X CN( -N 1A 4rP, 3 R ~J i C 6 7IV~~T~)\-N(RD)CON(R)- (R'RTY I Ra t) s C-XW: CI 6 7/L: (_Si2N (R9)~A 1 (R9 Th 1-~~hU ;Y 7iJ5.-OR" 1 l" ZI± Cl- 6 7iLzkA'A, Rd C 1 6 777 WO 02/053523 WO 02/53523PCT/JP01111083
R
2 TR-Y R t R R U LY R 4
C
110 cllo DCi ~i'i- 7b Lfi 7 RK R2, RU R 4 Thi~ Ar -A'7 L7CR-S Ztfl07 L) 7 1) -YR3 k;5V L~t b~4 L(K) 0i)iJ~ A r T, 7 ri7 j 1 RXN 2 WO 02/053523 WO 02/53523PCT/JP01111083 9 -~~XffiCON(Rs)a,:Vt*-lp R 5
N:
C'b; M Tt LK. 6 tJT>&7 9 L fiT- X hM-N (RD CON (R 8 R3I~C 7)A tX R' N: -LT- T 5LLMT- UXSON(9 X ff79 I'S~4 A-79 IQ$2 4-f#IM1- 79 -Mq L 9-4~~v>ThrzK.6AM'L14 57 L- J6 WO 02/053523 WO 02/53523PCT/JP01111083 Ara Ale)~ TPFh i l6h3AV 1{7W: 2 %LLQ)ODV N,7 -Y-4-f-V Zz> £1 Zz6 1)5 U L, t5 W/I M 7I ZW,--L A I -i U9 L 0D-5 P q Y LfN1 1 ~TtI t 1 L ff II AT- flyfiI R 2 *-ARA (Dr *Ng t b g WO 02/053523 PCT/IP01I11183 9 y A-I' i/kr K j t- 7 U~7 7" 1 /IMi WO 02/053523 WO 02/53523PCT/JP01111083
OH
Nio a~l OH TplO Tp22 R' Rio H H Me H Me Me iix 0
OH
x Tp3O -NHCONH- Tp4O -So 2
NH-
Tpl5O -CH 2
CH
2 TpI80 -para-Ph- Tp190 -rneta-Pb-
OH
01N( 0
OH
R
R X Tp5O tert-Bu -CONH- 'Tp6O CF 3
-CONH-
Tp 155 tert-Bu Tp170 tert-Bu -N
OH
0 1 0 N'O
N
Tpl8 y 0N Jc
H
R' R' H H H Me Me H Tp93 n Y 1 OH 1 cl 2 OH
OH
~0
N
R 4 Tp 160 H Tp175 isoPr Rl y Tp14O H OH Tpl4l H OMe Tp145 Me OH Tp146 H NHNH 2 Tp149 H H Tp200 0 Tp2lO S 17 /N OH z TP250 -CH=CH- Tp26O S WO 02/053523 WO 02/53523PCT/JP01111083 J_12 AR:4 MV) P- P 4FI{ Lz-i fli7) 7V- 7 1 tD& 1C RI M 2--CIO v A-N~ L~ U C J 43 U '9t*3 m DFA i ,101 WO 02/053523 WO 02/53523PCT/JP01111083 ttAl-ft AtIrW ql 7 1LA" MRA, A Rut rA i A Q A 4 A R t r-,l i X R q- M 0 T 6 D ff M T PPI &I f P ICI h, VI J CF, T p 0 5 0) WO 02/053523 PCT/JP01111083 OH OH OH 0 NaNO 2 IN Pt0 2 I H 2 ONO C) 9501 H 2 N I-i 1-2 OH OMe 1) NaNO 2
IH
2
SO
4 1)Tf O I 2,6-lutidine 2)A 44% H 2)MeOH/Et 3 N 34% TfO 1-3 1-4 OMe OH )n-BuLi IZnC1 2 0 NaOH 0 2) Pd(PPh 3 4 I 1-4 i31% I 52% 15 12 t 4. 54 g (37. 2 nmol) i'FI 12 il, 7 4 nl U, )JMzl, q A b 9 r 3. 72 g (53. 9 nmol) 8 ml Ut T Mr=t-t I-1 MR1I)A 5. 03 g (90 ~i~Ji- 4L-~'I-1 '11-NMR (400 MHz, DMSO-d 6 30 OC) 13.92 1 H1), 7, 70 J 12. 4 Hz, 1 7.22 J 11,7 Hz, 1 6.56 J 12.8 Hz, 2 H) 0 I-1 5. 00 g (33. 1 mmol) j/ 3 50 m 1 U Pto 2 40 m g JJ n -t A 7X U PC 2. 5 04 rml:R FZ T, i b~5 iL 7) Mt&J 5 00 m g )J n t bNigJ U, t 4L-MA4 1-2 OfLJgjt 4. 30 g (95 T) 'J 1-2 'H-NMR (400 MHz, DMSO-d 6 30 OC) 7. 10 (dd, J 10. 6, 1. 3 Hz, 2 6. 71 (dd, J 10.6, 1.3 Hz, 2 6.23 2 H) 0 'f-ilt 1-2 1. 99 g (14. 5 mmol) L* 50 ml, W%61W 22. 4 ml i"-NNY t, 0 OCi.
-C F-A 17 J-,71(M' 1. 20 g (17. 4 mmol) -7Jh 5 ml T t, Pa OD;L- VZ r fC- 3 0 3 t P 2 r' )5 IA UIt U, 7HzX-0 ;t M APJ~34i 836 nig (42 H-NMR (400 MHz, DMSO-d 6 30 0 C) 10. 24 WO 02/053523 WO 02/53523PCT/JP01111083 1 7. 15 (dt, J= 11. 7, 1. 3 Hz, 2 6. 96 (dd, J= 10. 4, 1. 5 Hz, 2
H)
0 4L-Pr*JI 1-3 420 mg 04 mmol) RU 2, 6A 9>0. 85 ml (782 mg,. 7. 30 mmol, 2. 4 A) ;L If L- 5 nil ;VP -30 0 C~7 F 9 7/1-,t1 r(TFA) 1.-8 9 g 70 nmol1) '51 ft. 3. 5 t- 7j(P U-i tt, f ppwLj 115 ml LW U, 9 c A,'7 1 ml ;L-D>C- -(Ir 41 ;0 C fW) 4 TL 4 25 8m g (3 4 tl 1 PC.Lf-L AIM I- 4 H 'l-N MR (400 MHz, DMSO-d 6 309 0 7. 45 (dd, J= 12. 9, 2. 9 Hiz, 1 7. 39 (dd, J 10. 7, 2. 9 Hz, 1 7. 10 j 12. 9 Hz, I 6. 93 j 7Hz, 111), 3. 3 H) 2 6, 7,8- F51% t 5, 5, 8,8-i xT-]~7 7 32 8 mg 23 mmo)~F L Fi27 7(THF) 3 ml t, -78 0 Cil7 -n-BuLi 1. 6 M S0. 92 ml 48 no) jjfM4-, 3 i 0 3 *L P: DMTL A ED 168 mg 23 nmol1) THF 2 ml L b L 4- fU-gL t 1 W5 $1 1-4 220 mg 82 mmol) RUPd (PPh,) 1 71 mg 062 mmol) THF 5 ml K2hjU)Jfl, Ri1LUi. 4 04m* 71 iifl*-, ffl R- T'FlU, JL-j 1-5 5138 mg (52 1 T 5: 'H-NMR (400 MHz, DMSO-d 6 7. 55 (dd, 1 HI, Pd (PPh 3 4 L 7. 47 J= 2. 2 Hz, 1 H), 7. 40 J 3 Hz, 1 7. 37 (dd, J= 10. 3, 1. 7 Hz, 111), 7. 30 (dd, J= 8. 1, 2. 0Hz, I 7. 11 J =12. 7Hz, 1 7. 07 J =10. 5 Hz, I1H), 7. 07 J =10. 5 Hz, 1 3. 87 4H1-), 1. 66 411), 1. 29 611), 1. 26 WO 02/053523 WO 02/53523PCT/JP01111083
H)~
4L-A 1I-5 130 mg 40 mmo) n2-/L- 6 ml iL 1 2 N7JZ Lt h9 A 3 m I Ut.~ 15 j 2 Nt E 4 L T pO05 3 8 m g 31 14 L-ft T p 05 FShr 161 0 C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 64 J 11. 7Hz, 2 4. 78 J =2.O0Hz, 1lH), 7. 40 J 3Hz, 1 7. 30 (dd, J 3, 2. 0Hz, IH) 7. 27 J 11. 7Hz, 2 H) Anal. Cal cd for C 21 2402 C (81. 78 H 87% Found C (81.57 H)I (7.87 IN 2 :4L- TplO 6)'j)3 OH1) NaNO 2
/H
2 S0 4 OH 1)TW 2 2,6-lutidine e HN0 2) K1 71% 2) MeOH IEt 3 N 43% 1I> 1-2 11-1 11-2 N211-2 Pd 2 (dba) 3 BINAP a-:O H ODC8 2
CO
3 Me quan OH 11-3 TrPIO t/N"4 1-2 5. 38 g (39. 3 nimol) ,A E 21 ml i U, j 30 g -MAPt 0 '0:CRfl 1' 9 r7A 2. 98 g (43. 2 nimol) 15 ml DC4i3 1- 30 3Th1AL7' Uft L, E4l 9 r Ab 71. 7g (432 mmol) ~7(90 ml- nW~ t Lk-- M9STJ04K4L -C 1-r% t rAaU 3.454gg (t6. 90 g, 71 jaH4t. -t 1 11-1 'H-NMR (400 MHz, DMSO-d 6 30 9C) WO 02/053523 PCT/JP01111083 7.83 J 11.9 Hz, 2 6.81 J 11.7 Hz, 2 H) tf-'M ilI-1 300 mg 21 mmol) Xt 2. 0. 11 ml (97 mg, 1. 45 mmol, 2. 4 i A) {L/VL L, 3 ml ON U, -30 'CT 7J TFA 375 mg 33 mmol) 2 04Y -Ctt W U, -hV, -J 2 Nf.M INTJU MgS0 4 C L U~O+~ k--J 2 C-PR 4LL 11-2 135 mg (43 C-i47':. {L6 00 11-2 H-NMR (400 MHz, DMSO-d, 30 0 C) 7. 75 (dd, J 10. 3, 1. 7 Hz, 1 H), 7.63 (dd, J 1.7 Hz, 1 6.65 Jz- 12.7 Hz, 1 6.60 J Hz, 1 3.81 3 H) 0 ti8'i 11-2 310 mg 18 mmol). 2-7 6, 7, 8-5p F tt 1- V1L 5, 5, 8, 8- F f/ Iv -t 7 Vr 1-2- 240 mg 18 mmol) HlM1r z-,A 463 mg 42 mmol) 2. 5 mol Pd 2 (dba), 27. 1 mg 030 mmol)., racemic BINAP 81. 0 mg 13 mmol) 7k ~JR C, k~ -Clt M UI L, AWN ~~~~~ttkTi~L 'IMgSO, U it f -ki el E A L 7 Y t Y) L- t a s~F 3~7 f ~ii5~ L 1 it, j= 4 0 1 T, rR II-3 98 mg (19 11-zr73 'H-NMR (400 Mh-z, DMSO-d 6 30-C) 8. 51 1 7. 27 8. 5 Hz, 1 7. 15 (dd, J 13.2, 2.7 Hz, 1 7.02 J 13.0 Hz, 1 6.94 (da, J 8.5, 2.2 Hz, 1 6. 93 J 11. 5 Hz, 1 6. 55 (dd, J 11. 2, 2. 7 Hz, 1 3. 71 3 1.64 4 1.24 12 H) 0 t-LA- II-3 90 mg 27 mmol) ;k 47 HBr 5 ml i ll AL-7'U 9 Wr't WO 02/053523 PCT/JP01111083 DtcL*, APR L ll~' TplO 94 mg (quant) 'fL-2}3 TplO it, Hk A (-r37 L-A) ;iAIk, 216 'C H-NMR (400 M liz, DMSO-d, 30 0 C) 8. 58 1 7.28 J 8.3 Hz, 1 7.16 (dd, J 12.2, 2 7.03 J 11. 5 H-z, 2 7. 02 j 2. 5 Hz, 1 6. 94 (dd, J 8. 5, 2. 5 Hz, 1 H), 1.64 4 1.23 6 1.23 6 H).
IJ3 4 Tp20 XY Tp22 0-8-)t
H
2 11-2 Pd 2 (dba) 3 BINAI'>o H Br Cs 2
CO
3 50% OMe quan OH In-i Tp2O NaHCH 3 148
CH
3 CH 3 0 O HBr a OMe qa OH 111-2 Tp22 T 11-2 158 mg 60 mmol). 2-7 2-5, 6, 7, b 1L I!r2-3, 5, 5, 8, 8z -A-t:7 t7 1I/-7 131 mg 60 mmol) PeRMt zr 7 236 mg 72 mmol), 2. 5 mol Pd 2 (dba) 3 13. 8 mg 015 imiol). racemic BINAP 41. 1 mg 066 mmol) 1 7 J( t-/ZY 4 ml t 100 0 C -{Tt 4L, O 5 rf 3l Ki R DL 2-A- 4 0 1) I CI~ 4L--qqZI11-1 129 mg (50 %)ji 4-II1 'H-NMR (400 Mliz, DMSO-d 6 30 0 C) 8.14 1 7.21 1 7.11 (dd, J S13.2, 2.2 Hz, 1 7.02 1 7.01 J 13.0 Hz, I 6.91 (d, 11. 2 Hz, 1 5. 91 (dd, J 11. 2, 2. 4 Hz, 1 3. 66 3 2. 09 (s, 3 1.63 4 1.24 6 1.20 6 H).
WO 02/053523 WO 02/53523PCT/JP01111083 111-,' 1 125 mg 36 minol) t- 47 HBr 6 ml M U, Mru t" 4~h~bU MgSO 4 V~fi Utk ukr 4LA--* Tp2O C91AIfKA 131 mg (ciuan-b) MA4 mO4LtI VW L ffA5166 9C 'H-NMvR (400 MHz, DMSO-d 6 0 C) 8. 28 11H), 7. 21 1 7. 15 J 12. 2 Hz, 2 7. 04 1 6. 72 12. 2 Hz, 2 2. 09 111), 1. 63 411), 1. 25 611), 1. 30 6 H) ;Anal. Calod for C,,H 27 N0 2 1/4H 2 0 C (7 7. 2 7 H 11 N 10 Found C (77. 37 11 02 N 12 9) NaH 60 in oil 16 mg 43 nmio)n MAL_~- DMF 1 ml VN Uit 0 111~-ji l-1 100 mng 28 mniol) DMF 2 ml 1,~ i af~z tTR4Utt 0 2031k n rY r4L AA- 0. 1 ml t-J -C2 1 f A -A-40 :1-20 1) TM t, fL-A*1 111-2 70 mig (48 ?l~ft,, {L~?j111-2 H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 28 1 7. 03 1 H), 7. 01 J~11. 3 Hz, 1 6. 89 J 13. 4 Hz, 1 6. 72 (dd, J= 13. 4, 2. 9 Hz, 1 6. 22 (dd, J= 11. 3, 2. 9 Hz, 1 3. 72 31H), 3. 18 3 2. 04 3 1. 63 4 H) 1. 26 6 1. 19 6 IM -1t 111-2 65 mg 18 mmol) 47 HBr 3. 5 ml L, A L Lit 24 T'LLfA eptW Uif. 4L-A4 Tp220 f lJ-5-IA66 ing (quant) L4 L- JL -PA Tp22 J jr.V 168 0 C H-NMR (400 MHz, DMSO-d 6 30 0
C)
7. 29 7. 14 IJ 12. 4Hz, 2 7. 05 11H), 6. 65 (di, J 12. Hz, 2 3. 19 1 2. 03 3 1. 64 4 1. 26 6 1. 19 6 H) Anal. Caled for C 23 11 2
,N
1 0 2 C (78. 60 H 32 N 98 Yo) Found WO 02/053523 PCT/JP01111083 C (78.47 Ii (8.41 N (3.92 IJ4 :4L Tp30 OD OH OTs TsCl /t 3
N
H
2 N 45% HN 1-2 IV-1 COOH1)SOC1 2 1)L\N 2) NaN 3 2) Py I IV-1 OTs 87% 9 IV-2 19% IV-3 NaOO Tp3O Il=~i~ I-2 250 mg (2.07 mmol) :4Hrid-, Lz 5 ml kr U\ F' rl ~5i 4F473 mg 48 mmol), ~~rF1 7IZ~1m fai 7z J -P'f Ail*~f7L C'E±i..U Y7 MgSO' -C~rr~l L, tt-'t j I-1 245 mg (46 j 'H-NMR (400MHz, DMSO-d 6 7.77 J 8.3 Hz, 2 7.41 J 8.5 Hz, 2 7.22 2 H), 7. 05 J 11. 2 Hz, I 6. 98 J 13.2 Hz, I 6.96 (dd, J 13.4, 1.7 Hz, 1 5.92 (dd, J 11.2, 2.0 Hz, 1 2.40 3 H) 0 6, 7, trl~ 51 5, 8, 8-5 9 11 7 3rL 27 /iR; iE 500 mg 16 mmol) Zz1 5 ml, it- 2. 56 g 1,710, X L, j sUi LO" 2 RUrpif A, VA J71 F- 5Uni l L, 7 4l t f 9 r 7 238 mg 66 mmol) 7J( 1. 2 ml G U-fiCV -C 35'-40 0 CI 30 351R4 Lk'. ZJ~JI WO 02/053523 WO 02/53523PCT/JP01111083 {L~IV-2 :'H-NMR (400 MHz, DMSO-d, 30 0 C) 7. 89 J 2. 0 Hz, 1 7. 68 (dd, J8. 3, 2. 0 Hz, 1 7. 51 if8. 3 Hz, 1 1. 66 4 1. 25 12 H) 0 f L-6'10z TV-2 206 mg 80 mmol) 3m1 &6 L, 3ii~bLIt. 2 PirpliI, R U, 4LI-K- IV-1 200 mg 69 mmol)*2/7'T /O9 (DMAP) 8.9 mg(0. 072 mol) %5NU2~t 20 Wff' P!:U 7J<.LJl.
-CU, WU, T>F LIA L24' U, 7MfUL~ A Ahc-c--&h "Jr1 MgSO 4 TIO I, C-Ait IV-3 68 mg (19 J-t JLm IV-3 :'H-NMR (400 MHz, DMSO-d 6 9. 27 1 8. 81 I 7. 80 J 1 Hz, 2 7. 50 (dd, if 11. 7, 1. 9 Hz, 1 7. 45 j 8. 5 Hz, 2 7. 38 J 1. 9 Hz, 1 H), 7. 37 (dd, if= 16. 8, 2. 5 Hz, 1 7. 34 J =11. 2 Hz, 1 7. 23 Ji= 12. 6 Hz, 1 7. 16 (dd, J= 8. 3, 1. 9 Hz, 1 7. 14 Jf 13. 2 Hz, 1 H), 2. 42 H1), 1. 62 3 1. 22 6 1. 21 6 H) 0 ILV- 13 60 mg 12 mmol) 7Jf4tbJ7A 40 mg 12 ml 71J YI L L ~hU, A -V IUft.
0 6 NNi 60 OC 9 7j(, EET W U-C %2 N:W&C'PH 5-5.0 ZU NIj<,,A fVT*?"7J(TCAV '1 MgSO 4 V U1%t7-A L 7:7 'y 'YV' r Y' 4 z A- U, 4L-to
T
p 3 O 25 mg (59 t 4fL-W^-t Tp3O 0/s ~L 207 'C 1 H-NMR (400 MHz, DMSOd6, 30'C) 8. 78 1 8. 59 1 7. 57 J =12. 2Hz, 21H), 7. 37 (d, Ji- 2. 2 Hz, 1 7. 22 if= 12. 2 Hiz, 2 H1), 7. 20 if= 8. 6 Hz, 1 7. (dd, Jif 2. 2, 8. 6 Hz, 1 1. 62 4 1. 22 6 1. 21 6 H) Anal. Calcd f or C 2 2 11 2 6 N_0 3 1/2H 2 0 C (70. 38 H 25 N 46 Found C WO 02/053523 PCT/JP01111083 (70.32 H (7.21 N (7.37 Vq 5 :4L8-tTp40 OH OMs MsC /Et 3
N
H
2 N 45%H 2
N
1-2 V-1 OMs om CtS03H SOcl pyridine! V-1 o., 98% 12% V-Z V-3 NaOH quant 0, O Tp4O 1-2 1. 00 g 30 mm1) 2AI4 J 1- 10 ml t L. F F A7 1. 5 ml, Zi Pl2 -f 1-836 mg 56 ml, 7. 30 mmol) ONarT, 1L U ft.L~z 2 8 F rpl ig A 'R 7 y 9 Y; 7FJ t 13; J, 3 7 4 4L--t V-1 828 mg (52 IiP. L V-1 'H-NMR (400 MHz, DMSO-d 6 3000) 7. 29 (bs, 2 7.24 (dd, J 12. 2, 1. 0 Hz, 1 7. 13 J 13. 2 Hz, 1 7. 02 (dd, J 13. 2, 2. 0 Hz, 1 6. 02 (dd, J 11.7, 2.0 Hz, 1 3.33 3 H) 0 3 tlA;L-7 A- 2. 0 ml 0 OCIC 1, 2, 3, F H 1- V 1, 1, 4, 4-7i 7( ~A-'t7 Yr 1. 00 g (5.32 mmol) I)J-~x tJ 1 kk7j(,1.
V-2 ~$hItY 1. 50 g VI~i~ {-1i V-2 'H-NMR (400 MHz, CDCL 3 7. 93 J 2. 2 Hz, 1 7. 74 (dd, J 8. 6, 2. 2 Hz, 1 7. 52 J 8.6 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 1 11), 1. 73 4 1. 33 6 HI), 1. 32 6 tLp'L140 V-I 200 mg 93 mio1) 4L',j-IW V-2 267 mg 93 inmol) -PIIzJ. tf1)~ -3ml iLAAU rETA ~i Uk 0 2 *Ir1l~k 7JQJ-fZ. 7 -q SL N WR WP-fi*-% MgS 4 %%Uk ,AM Uft. Y i A Yr, 7 7-f- (WFR-XV) -0OH 1- L-M'"V-360 mg (12% {L-4PC .tt; V-3 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 10. 94 1 7. 73 (s, I1H), 7. 58 2 11), 7. 51 J =10. 7 1z, 1 i1), 7. 30 (dd, J =13. 5, 2. 7Hz, I 7. 21 J= 13. 2Hz, il-1), 6. 89 (dd, J= 10. 9, 2. 7Hz, 1 3. 42(, 3 1. 63 4 1. 22 6 1. 20 6 HL~ 4L-V'i V-3 45 ing 097 imo) Y2--37,'-'I3 ml, 2 N7J3' fb~ t 1 ml U~h k U7 6 VTrliJ! 2 N AM-- t L L 4 t SMgSO 4 ,C*,1P-A SA~tf. tmL Tp40 -)fI~Ut 6 211 9C 'H-NMR (400 MHz, DMSO-d., 3000) 10. 11 1 7. 53 (d, J 2 Hz, 1 7.561 J 3 Hz, 1 7. 44 (dd, J 3, 2. 0 Hz, 1 7. 13 J= 12. 2 Hz, 2 7. 19 J= 12. 5 Hz, 2 1. 61 411), 1. 21 6 1. 13 6 H) Anal. Calcd for C,,H 2 BNlO 4 Sl C (65. 09 H1 50 N 61 Found C (64. 84 H 47 N 69 16 C4~Tp50 O-A- 0 0 R0
OH
R COCd DMAPI-I R 0 0 0aH RQ N0 IN
H-
H 0) 0pyridine
RR
VI-1 (R =tert-Bu) VI-Z (R =tert-Bu), 92% Tp5O (R tert-Bu), 42% VI-3 (R CF 3 V1-4 (R CF 3 80%/ Tp6O (R CF 3 5 3%O WO 02/053523 WO 02/53523PCT/JP01111083 3, APf 550 mg 00 mniol) bl MOIUtc-' 1- WI? V VT-i :L-81t 1-2 158 mig 15 mmol)~ 10 ml, DMAP 1 )t 9T4 zk A- N JM 4 U 2 1) -Ct&L 4E7 -410VI-2 600 mg 4LIV-2 600 mg 05 mo:1- r -'10 ml -c'5 A 4LAF 2.10 ml fl -Lti j2 Nt 30 ml i- PH 2 L O T U A FtW4 9p Lft 0DS7, F 74 ,L -v (th9 A- 2 1 J -rr, L, 4L- 1IV TpSO 149 mig (42 K4JTp5O 2 9 f2A (lA4L' 236 0 C;Anal. Calcd for C 22 H,,N,0 3 C (74. 76%/) 1(7.70 N(3. 96 Found C(74. 56 H(7. 63 N(3. 82 INJ7 :4 3,5-1 :7 9 7 I 1KfL V VI-3) 560 mg 02 nimol) 4l VA 1-2 137 mig 00 mmo)~ If 9 $-z5 ml, DMAP 1 it -hfl X -Al 2 1) -C UX4Lg VI-4 500 mg (80o1/) L-~~iVT-4 H-NMR (400 MHz, CDCT 3 9. 00 1 8. 47 2 11), 8. 39 21H), 8. 12 11H), 8. 03 11H), 7. 70 j =12. 1Hz, 21H), 7. J 12. 1 Hz, 2 H) {L~VI4 500 mg 81 imo) =5 7/ -AL6 ml 4)F9 ~Y~3 ml li1~i t- 7" L z.S 4rA-' 2 N 3 0 mi WO 02/053523 WO 02/53523PCT/JP01111083 PH 2 L 51 -UF 9 t,, L Tp6O 160 mng (53 f {L'AI Tp6O X j7C, RwVA149-150 0 C 'H-NMR (400,MHz, CDCl 3 8. 33 2 8. 09 1 8. 05 I1 7. 71 J= 11. 3 Hz, 2 7. 38 J =11. 5 Hz, 2 H) Anal. Calcd f or C 16
HN
1 0 3
F
8 C (50. 94 H 40 71 Found C 87 H 70 N 44 0118 4L121 Oj Tr)8 0, Tp 8 2 Y T p 8 4 1- A 0 CO1)SOCI 2 N iili1 1)4 H 0 Oa2) pyrine( DMAP 11-2 -0 82%
VIM-
O 0 1) NaOH 0 N aH0 O 2) Ac 2 O/pyridirie w H I W H 9%VU-2 Tp8O 1) NaHl 2) CH 3 I, 660k O 0 0 fAc 0 H N!O N w~ I wI VIU-3 Tp82 6, 7, 8 Vh1r5,,8, h 92vfrAt7 2 /'rX7 00 g 2 mmol) A A-18. 0 g, 20 ml P-MU 1 1AR9MI UP-, 2 *-pjMWiMt 5-7 17ThZ2. 07 g (15. 1 nniol) t-V It, 41 7 J(h' 9 $f-9 20 ml iIL DMIAP 100 0 C-CRO Uft 1 UV, C#MU 2 N AR MfPth -C N MgSO 4 WO 02/053523 WO 02/53523PCT/JP01111083 44Wz~zz 1 -2 0) Tri UL-Pt1 VII-1 6. 96 g (82 %~t 0
'L
i~VII-1: 'H-NMR (400 MHz, CDC1 3 8. 13 J 2. 0 Hz, 1 7. 98 1 H), 7. 90 (dd, J 8. 3, 2. 0 H-z, 1 H1), 7. 86 J= 2. 2 Hz, 1 7. 56 (dd, J= 8. 3, 2. 0 Hz, 1 7. 41 J= 8. 3 Hz, 1 7. 40 1 7. 38 J= 8. 3Hz, I1H), 7. 29 (bd, J11.7 Hz, 21H), 7. 29 I1H), 1. 72 8 1. 33 6 1. 32 6 1. 31 6 1. 29 6 H) 0 ML-'I~g VII-1 6. 96 g (12. 3 mmo) ml, z-W-A,40 ml i,.
_4 L, 2 N &1 4K hJ 57 A 3 0 ml lk)Jn RTR P 2 0 rp 2 N :tR fR'iL Uf, ;Ah'S I O U t-W ji~~ MgSj i1--t t 7. 35 g (quant. 6D*1-" 6. 43 g ,u 7J(.e 9 2 '0m 41 Ill- i3 0 m1 I 'L7 7 tJ 2 F1{ 4 m k, A/ 4A~zz 1 3 -LC--rj t 'fL tA- VII-2 4.12 g (95 Y) O tE-N't VII-2: 'H-NMR (406 MHz, CDCl 3 7. 87 (br s, 1 7. 84 J= 2. 0 Hz, 1 7. 54 (dd, J 8. 3, 2. 0 Hz, 1 7. 53 2 7. 43 j 3 Hz, 1 7. 23 J12. 0 Hz, 2 2. 34 3 1H), 1. 72 4 1. 34 6 H) 1. 31 H) 0 t-ISA'A VII-2 4. 12 g (10. 5 mmnol) 9t-L V zZ- 50 ml,-r3 40 ml 74 1 U, 2 N~jT~ hf''tt 9 40 mil T3D-Wl 0 n 2 Oji1j 2 N J t, ft% f U -C Tp 80OD R- ZV 2. 9 0 g (9 1 ;LIi t Tp 8O0:t" j YplY A 3t 1 rRIVA 209 0 C 1 INMR (400 MHz, CDC1 3 7. 83 J= 2. 0 Hz, 1 7. 73 1 7. 71 zJ 12. 3 Hz, 2 7. 54 (dd, J 8 2 Hz, 1. 8 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 111), 7. 42 J 3 Hz, 1i 7. 36 j =12. 1lHz, 2 1. 72 (s, 411), 1. 33 6 1. 31 6 H) Anal. Calcd for 222,,N3 C (7 5. 19 H 17 N 99 Found C (75. 24 11 27 Yo) N 90 NaH (60 31 mg, 0. 76 mmol) 1i\CV DMF 1 ml LUiUf, ~~f-~IJVII-2 200 mg 51 mmol) -ar DMF 3 ml L) 7Ct, MC- 1, t. 5f& E r ~4L 1-/1J0. 1 ml ;EN% Lft 30$~ 3 7J t I-'~97 1 I) -Cr- JUC 4Ej-;t1K VII-3 136 mg (66 ;Ifl {Ko S1V VII-3: '11-NMR (400 M H-z, DMSO-d 6 300C) 7. 32 J= 8. 1 Hz, 1 7. 26 (dd, J= 8. 1, 1. 7 H1z, 1 H1), 7. 16 J= 12. 2 Hz, 2 7. 13 J= 1. 7 Hz, 1 H) 7. 10 J= 11. 7Hz, 211) 3. 35 31H) 1. 55 4 H) 1. 18 611) 1. 01 6 E)~ 'L VII-3 133 mg 33 mmol) ~zu 8 ml U, 2 N *M4'L JiW~~bU/O ~ni(CM "MgSO 4 V+I~L U7r. 'f Uc.
Tp82 MR t RM 120 mg (quant.)Itc Tp82 L 2 94 C 'H-NM4R (400 M Hz, DMSO-d 6 30 0 C) 7.28 J 8. 0 Hz, 1 7. 27 12. 0 Hz, 1 7. 20 (dd, J= 9. 0, 1. 7 Hiz, 1 11), 7. 07 J 7 Hz, 1 7. 01 J- 12. 0 Hz, 2 HI), 3. 32 3 1. 53 4 11), 1. 16 6 0. 97 6 H1) Anal:' Caled for C 23
H
27
N
1 0 3 1/41-120 C (74. 67 H 49%Y) N 78 Found C (74. 91 H 58 N 71%) 6,7, 8- b F 5, 5, 8, 3- -F V-7 -;Z -C TOSO L U -C Tp84 U L, Tp84: (L WO 02/053523 WO 02/53523PCT/JP01111083 z) AR 206 0 C 'H-NMR (400 MHz, CDCl 3 7.72 J= 12. 0 Hz, 2 HI), 7. 45 (bs, 1 7. 41 1 7. 37 J 12. 0 Hz, 2 7. 1 2. 46 3 1. 70 4 1. 30 6 1. 29 6 H) Anal.
Calcd for C 23
H
27 N0 3 C (75. 59 H 45 N 83 Found C (75. 49 H 50 N 64 06 9 tL-tTp88 016' 0) t{L A-45t ',Tp8 8 4L-. Tp8 8: ~I'~142 cC 2 11-NMR (400 MHz, DMSO-d 6 30 O(D) 10. 16 1 HI), 7. 83 (dd, J=8. 6, 2. 2 Hz, 1 7. 73 J= 2. 4 Hz, 1 7. 72 J 12. 2 Hz, 1 7. 22 J 12. 2 Hz, 2 7. 08 J 8. 8Hz, 1 3. 88 3 H), 2. 0 7 6 H) 2. 0 5 3 1. 74 6 H) Anal1. CalIecd f or C 25 H1 2 7N 1 0 4
H
2 0 C (70. 90 H 90 N 31 Found C (71. 19 H 94 Yo) N 31 04 107 Tpi 6 D/V\4L TpO {Kt~Tp9O J( (J 149 0 C 'H1-N\MR (400 MHZ, DMSO-d 6 30 10. 23 1 H1), 7. 82 J 12. 2Hz, 2 7. 56 J= 15. 6 Hiz, 1 7. 56 1 7. 34-7. 42 (in, 2 7. 25 J= 12. 2 Hz, 1 6. J15. 9 Hz, 1 3. 65 4 1. 27 6 H1), 1. 25 6 H) Anal.
Calod for C 24
H
27
N
1 0 3 -1/4H 2 0 C (75. 46 H 25 N 67 Found C (75. 47 H 31 N 59 Yo).
WO 02/053523 PCT/JP01111083 Cl SCOH 1)SOC1 2 N 2) pyridinef DMAP I TV-i H 9.2% Tp93 6, 7, 8- F t fl-5, 56,8, 8-5 VI -A -A'±73 L- 2-f 77 91 11-R 355 mg 45 mmIol) 1,l~krh~-IV 1. 73 g, f 5 mI LDJJ L, M it UfL 2 Wfilfk, UL 'j IV-i 400mg 45 mmol) j 7 9j l 5 ml i5m tL- DMAP 53 ing 44 immol) JJP 100 'C -C"Itit Lt JA, 7ffl ut-iil-U 2 N MgSO T' Uk L IC Ah i~f L, Pt. 9 YA- t Y b, rl -7 3 Y 7 i' 7 (ffrki zlt A- Zz 1) TOW UN RItTp93 48 mg -kil~fc 4L' it Tp93 17 9 ZC.A Fi- iI 241 9C 'H-NMR (400 MHz, DMSO-d 6 10.05 1 7.99 J 11.0 Hz, 1 7.91 (dd, j 11.0, 2.2 Hz, 1 7.60 J 16.1 Hz, 1 H4), 7.58 J= 2.2 I-z, 1 7.55 (dd, J 13, 2, 2. 2 Hz, I 7. 36-7. 42 2 7. 24 J 13. 2 Hz, 1 6. 78 J 15.7 Hz, 1 1.65 4 1.27 6 1D, 1.24 6 04J 12 4UP9it Tp95 OD -083Z E) 6, 7, 8-5 t i 5, 8, 8- F7 3r 1, -2--f 3 li 4 -W PP U-C I 6 tV4 t L Ut. 4 t Th Tp95 'A%97 9 XA 216 'C; 'H-NMR (400 MHz, CDC1) 7. 71 J 11. 9 Hz, 2 7. 53 (dd, J 10. 8 Hz, 14.9 Hz, 1 7.29-7.37 5 7.18 (brs, 1 6.95 J 15.2 Hz, 1 6. 85 (dd, J 10. 8 Hz, 15. 4 Hz, 1 6. 04 j 14. 7 Hz, 1 1. 4 1.31 6 1.29 6 H) 0 WO 02/053523 WO 02/53523PCT/JP01111083 Od13 :4L-'-it Tp140,. Tpl4l R jY Tp145 6D8- By r 'mS- -/Pd(PPh 3 2
C
2 I j Et 3 N Cul 79 Ts
K
2 C0 3 0 94% V111I.1 VITI-2 Pd(PPh 3 2 C1 2 I CuIi /Et 3
N
11-2 81% 4141l
NH
2
NH
2 1 NaOH qtiant
TH
2 6.6% Tp14O Tpl46 Tpl49 OMe Tll Pd/C/H 2 I 0 NaOH 86% VIII-3 Tp150 2- i/ 12-- 5, 6, 7, b 11-5, 5,8, 8-t~ b I77y 3. 00 g (11. 2mmol)R-OQ, 1"fLMR237 mg l2nimol) T.z$T 225 ml ~Ch~~c~~TO -7-t zH- 3. 31 g (33. 7 inmo) /tr Pd (PPh)C1 786 m g(1. 12 mmo 1) 0 /4 7 0 'C 1 UIcO 2 2flT& P49~U f-.4 1 OR t t NH 0OH/ NH 4 C 9/ 1 7(X I 7R. N -W 4L--01 VIII-1 2. 51 g (79 4LjRj- VII-I 'H--NMR (400 MHz, CDCL 3 7. 40 1 HI), 7. 21 2 1. 66 4 1. 26 WO 02/053523 WO 02/53523PCT/JP01111083 6 1. 25 6 0. 24 9 H) 0 J'fK t VILE-i 1. 00 g 52 mmol) 31 15 ml L 9 Ah 97 mg 70 mmolI) 2VAT. i' 24 PRPMIR4O L7Jt ii*-f7'., 'f~tiVIII-2 700 mng (94 -6 -#AJ VIII-2: 'H-NMR (400 MHz, CDCL 3 7. 44 1 HI), 7. 26 2 3. 01 4 1.27 6 1. 26 H), 4tJ'jVII-2 136 mg 64 mmol)RV~fL-t 11-2 160 mg 61 mmol) kF 3 J5/7~J 6. 0 ml Ll Ti JI: XAL, ci Pd (PPhl) 2 C1 2 112 mg 16 mmol)BzRJM El L1I 30. 5 mg 16 nimol) )JIII%.
I1) ICMi Tpl4l 171 mg (81 t-4L TP141 (1WL /J 1- 94,A 139 OC; 1 H-MR (400 MHz, DMSO-d., 30 0 C) 7. J1. 7 Hz, 1 7. 41-7. 46 (in, 2 7. 37 J8. 1 Hz, 1 7. 28 (dd, J= 8. 1, 2. 0 Hz, 1 7. 02 j 13. 0 Hz, 1 6. 97 J 11. 0 Hz, 1 3. 89 3 1. 65 4 1. 26 6 1. 25 6 H) ;Anal.
Calcd for C, 4
H
26 01 C (83. 20 H 56 Found C (82. 93 H 63 {L-JA Tpl4l 125 mg 36 nimol) 8 ml, 2 N *JRb tt 3 4m 7) II* It 3 R 2 N 'L It i ,M 9-L- M fJV\MgSO 4 TitUA I-t-k fLAltTp140 ~123 mg (quant) t-ff0 4-8910iTp1 40 j4k*Xp~- O~li 182 'C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 53 J 11, 7 Hz, 2 7. 43 Jz- 1. 7 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 1 7. 36 J= 8. 1 Hz, 1 7. 26 (dcl, J 8 1, 1. 8 Hz, 1 7. 09 (di, J= 11. 7 Hz, 2 1. 64 41H), 1, 25 611), 1. 24 6 H) Anal.
Calod for C,,H1 4 01 C (83. 10 H 28 Found C (82. 83 H 42 4L L7(, T1p140 L[FIQP UMtKirTDl45 Rf-iV{L14T15:~ 791 go2 (JWL/ JI-' V :k JAA 137 "C 'H-NMR (400MHz, CDC1 3 7.62 (ci, J =12. 0 H1z, 2 7. 42 1 H1), 7. 30 J 12. 0 11z, 2 11), 7. 16 (s, 1 11), 2. 43 3 1. 68 (4 411), 1. 284 6 1. 278 6 Anal.
Caici for 024112602 C (83. 20 56 %)Found C (82. 92 H 73 'f14 JL it Tp 146 X'z Y Tp 149 Th) 4L-I1[ 9Tp141 332 mg 96 nimol). A2-)1/ 2 ml, 2 ml, 80 %L I-- /*TJI 2 ml OAA R6- 10 3 U/MOM U CtIp U 0l1)RIt' 299 mig (90 4:'ij 4Ltt I Tp146 :'H-NMR (400 MHz, DMSO-d., 30 0
C)
9. 19 11H), 7. 48 (dd, J =11. 5, 1. 7Hz, 1 7.41 (ci, J 7z, 1 H), 7. 36 (dcl, J=12. 2, 1. 7 Hz, 1 7. 32 (di, J 8. 3Hz, 1 7. 21 (cid, J 8. 0, 1. 7 Hz, 1 6. 99 J=11. 2 Hz, 1 6. 74 (di, 'j 12. 0Hz, 1 H), 00 (bs, 2 1. 64 4 1H), 1. 25 6 H4), 1. 23 6 H) tl- 1t Tp146 250 mg 72 nimol) :O 1 ml, 7J 4 ml i-,,AU Mfil~ )A L 04 L, 'L 2N t -flti7 1~\MgSO 1 4 WV ULtc A t V 7 b 2 A' 1 0 0 1) I U, Tp149 15 mng 6 {-4jTp 149: 'H-NMR (40 0 MHz, CDCL,) 7. 45 (di, 1. 7 Hz, 1 WO 02/053523 WO 02/53523PCT/JP01111083 11), 7. 30 J= 10. 7 Hz, 1 7. 28 J= 10. 3 Hz, 1 7. 22-7. 26 (mn, 2 7. 08 (dd, J= 12. 0, 8. 5Hz, 1 6. 97-7. 003 (mn, 2 1. 57 411), 1. 30 1. 28 6 H) 0 TP141 80 mig 23 mno) m-Y -IL,5 ml U, Pd /C 20 mg -tU%.Z C- Vh he, R L PC 2 q-RJA,1 4ii T 1~ rA M9 4 A 4' 2 :1I) -C-NJt 4L-ji-tVTII-3 35 mg (43 %o);L,4f/t -1VIII-3 :'H-NMR (400 MHz, CDCL,) 7. 23 J 3Hz, 1 7. 22 (di, J 11. 0 Hz, 1 7. 14 (dci, J =12. 4, 2. 0 Hz, 1 7. 00 J 2. 0 Hz, 1 6. 94 (di, J 8. 1, 2. 0 Hz, 1 6. 85 J= 10. 2 Hz, 1 6. 64 J 10. 5 Hz, I 3. 92 2. 83 4 1. 66 4 1. 27 6 1. 22 6 H) 0 4KIm VIII1-3 34 mng 097 inmol) 2 ml U, 2 N *Nj'4Lt 7 9 I I 1 m R aJ{ ?R-C't 4t Lft 12 V, RI 70 0 G 6 OTWUiP-UO 2 N ~r i -'~hU MgSO 4 "r TPl50O D~h 28 mng (86%)i1O 4L-'t1* Tpl5O (rI -A ij~i,~ 138 9C ;'H-NMR (400 MHz, DMSO-d., 30 0 C) 7. 29 J11. 5 Hz, 2 11), 7. 19 (di, J8. 3 Hz, 1 7. 12 (di, J =11. 7 Hz, 2 7. 05 J =2.O0Hz, I1H), 6. 96 (dci, j 3, 2. 0Hz, I 2. 70-2. 85 (mn, 4 1. 60 41-H), 1. 20 6 1. 17 6 H) Anal.
Calcd for C 23
H
28 0 2 .1/4H120 C (81. 02 1H 42 Found C (80. 85 Yo) H 28 i16 TLPi T15 5 OD#II WO 02/053523 WO 02/53523PCT/IP01I11183 204 0 C 1 11-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 60 J= 11. 7 Hz, 2 H7), 7. J 7Hz, 1fH) 7. 36 J 7 Hz, 2ff) 7. 16 J =12. 0Hz, 2 H) 1. 29 18 H) Anal. Calod for C 23
H
26 01 C (82. 60 H 84 Found C (82. 46 H 93 o 'fJ 17 4'9JTp160 O'j-)R
OH
NH
2 1) H 2 S0 4 NaNO 2 1~ N 2) NaGH tropolone 23% P0 2-7 T -5y,6,7, 8- F 1h-5, 5, 8, 8-:7 ;g 77 -97 10 2 mg 50 mmol) i 30 7)L1Y 2 ml W U L 7 '6 T Lt,, 7 70 ing, 712 ml 1 3f .L -C+PL-iUPt t 0) 10 %7A(RP% u/2 mnl *r-z 270 mg 57 mniol) kr-lUfrjf ;ft T- Z tZ Ar2P;-' -~Lt t OD S 7 F Y- t i-7 4 Y 7- P L-/WL 2? A 185 00 'H-NMR (400 MHz, CDOD) 8. 21 (dd, J 1. 6 Hz, 10. 7 Hz, 2 7. 90 J 0 Hz, 1 7. 65 (dd, 2. 0 Hz, 8. 4 Hz, 1 7. 49 (dd, J 1. 3 Hz, 10. 5 Hz, 2 7. 45 (d,J 8. 4 Hz, 1 1. 74 4 1. 37 6 1. 33 6 H) 0 {18 K T p 170 ODR' Tp17 0 j~r5ZU ft. 4 Lt'i Tpl17O0 iR1L-tkAJ RAt 199'-201 00 'H-NMR (400 MHz, DMSO-ds, 30 0 C) 8. 12 J =12. 0 Hz, 2 7. 71 J- 1. 7 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 2 7. 61 J= 1. 7 Hz, 1 7. 36 J 11. 7 Hz, 2 1. 35 (s, 18 H) ;Anal. Calcd for C 21 H,6NO, C (74. 53 H 74 N 28 Found C (74.38 H (7.80 N (8.19%) 3, f 9 4-4 -f >7O 0 y IfL r, I-, -C fY1 17 OD)& 4ft 'fL8Tp 175 jtLft 0 U c 4L/KTp 17 9 -A-'17k) Fj',A 5145 0 C 'H-NMR (400 MHz, DMSO-d 6 3000) 7. 91 J= 12. 7 Hz, 1 7. 88 1 7. 50-7. 55 (mn, 2 7. 35 1 7. 19 J= 12. 7 Hz, 1 4. 32 J= 6. 8 I-Jz, 1 HI), 1. 69 4 1. 32 6 1. 29 (s, 3 1. 28 6 HI), 1. 28 3 H) ;Anal. Calcd for C 2
,H
3
,N
2 0 2 C (76. 16 H 99 N 40 Found C (75. 88 H 96 N 44 t-l-t Tp180 6D-M Br I AIC 3 1) n-IuLi ZnC1 2 2) Pd(PPh 3 4 1-4 X-1 (para), 99% X-3 (meta), 78% OMe OH -NaOH :-o X-2 (para), 29% Tpl8O (para), 24% X-4 (meta), 43% Tp19O (meta), quant 2.0O0 g 58 mnol1) V 4L~1>10 ml I T 4 A 6 3 mg r Jft -0 7 P 4J7(4I R 1t,,9-,af ',W WO 02/053523 WO 02/53523PCT/JP01111083 lz '2A N J'~Y fl~~i\MgSO 4 (400 MHz, CDCL,) 7. 53 J 6 Hz, 2 7. 47 (di, J= 2. 0 Hz, 1 7. 43 J 6 Hz, 2 7. 37 J 3 Hz, 1 7. 31 (dcl, J= 8. 3, 2. 2 Hz, 1 1. 72 4 1. 33 6 1. 31 6 H) Anal. Calcd for C 21
H
24
N,
2 1/41,O C (73. 98 H 24 N 22 Foundi C (74. 11 H 27 N 28%) 4L-HI*j X-1 275 mg 80 mmol) t- TU1F 3 ml ~78 O n-BuLi 1. 6 M z 0 .60 ml 96 innol1) -Vt 30 ftE U1~ rt. -0 1LCn 109 mig 80 mniol1) t- THF 2 ml i~ ,L L V, 7 2V ft. 1 H; m 1%z fL t-f 1-4 152 mg 54 molX)kRUPd (PPh 3 4 46 mng 040 inmol) t- THF 4 ml ,f 6D~ O JI)a iI L, tt 4. 5 7jZNfl x 2 1Rgt: -L 07 2 -CfmU, f E'tX-2 91 mng (29 1M~ X-2 'H-NMR (400 MHz, CDCL 8 7. 66 (di, J 8. 3 Hz, 2 7. 60 (dci, J 12. 7, 2. 0 Hz, 1 7. 52-7. 56 (mn, 3 7. 33-7. 41 (mn, 3 7. 36 (cid, J3 12. 4, 2. 0 H-z, 1 6. 88 (di, J =10. 5 Hz, 1 4. 01 (s, 3 1. 74 4 1. 36 6 1. 33 6 H) 0 IE84X-2 85 mig 21 in o1) 8 ml 2 N 71 Nft I 9 I 7 J>.3 mlIf T 4 U t 6 H rjlf 2 N Mt-i- 0M-j- ~Ajl Tp180 20 mig (24 4Li-!Kz Tpl8O ~4~iik j ,212 9C 'Th-NMR (400 Mlz, DMSO-d,, 0 CD) 7. 73 (di, J= 8. 3 Hz, 2 7. 71 (di, J= 10. 8 Hz, 211), 7. 65 (di, J WO 02/053523 WO 02/53523PCT/JP01111083 8. 3 Hz, 2 7. 59 J= 1. 6 Hz, 1 7. 45 (dd, J= 8. 3, 1. 6 Hz, 1 HI), 7. 40 (dd, J 8. 0 Hz, 1 1. 67 4 1. 31 6 1. 27 6 H).
{~J21: JL- Tpl9O 01-d) 3- T ASF-W W$q U -CjI 20 OtVA L Tp 190 ;L M" A UPL.C A~ TP190O: (It*5k 140 9C 1
H-NMR
(400 MHz, DMSO-d 6 300C) 7. 75 J =12. 0 Hz, 2 7. 75 (bs, I 7. 63 (dt, J 4. 4, 7. 3 Hlz, ,I 7. 60 J 2. 0 Hz, 1 7. 53 J 4. 9 Hz, 2 7. 45 (dd, J= 8. 3, 2. 0 Hz, 1 11), 7. 40 J 8. 3 H1z, 1 7. 30 (d, J11. 8 Hz, 2 1. 67 4 1. 31 6 1. 27 6 {22 :4-1JTp200 OD-d SBr -~Pd(PPh,) 4 1) X in-BuLi /ZnC 2 +o (HO) 2 B X Na 2
CO
3 o 2) Pd(PPh 3 4 1 1-4 XI-1 (X X1-3 (X 42% X NaOH A X1-2 (X 19 Tp200 (X 155% XI-4 (X 4801 Tp2lO (X 2- 5 t 1 5, 5,8, 't tfi4 7~ -'57 V 3. 00 g (11. 2 imol) /'zXJ Pd (PPh 3 4 416 mg 36 mmo) =fT 2/ bz w 3. 6 ml t, 10 31M1MOL, Pt, 2--7 -ZJ '4Y 1. 45 g (12. 9 mmol) tbI1 1- iM~ 9rYb.6 M2 8 ml I bR1ijR n 5. 5 04l1-.k, 7 ~~rt\MgSO 4 UA Ltif{l riALT'f UfA b~7-f v~1:50)~4L~I-11.00 WO 02/053523 WO 02/53523PCT/JP01111083 g (35 t-14ki XI-1: 'H-NMR (400 MHz, CDCL 3 7. 61 J= 2. 0 Hz, 1 7. 44 J= 1. 1 Hz, 1 7. 42 (dd, J= 8. 1, 2. 0 Hz, 1 HI), 7. 31 J 3 Hz, 1 6. 58 J 3. 4 Hz, 1 6. 44 (dd, J 3. 1, 1. 1 Hz, 1 H), 1. 70 4 1. 33 6 1.,29 6 {LI~-1 497 mg 96 mmo1) t-THF 4 ml U, -78 'C C't- n-BuLi 1. 6 M 1. 84 ml 94 mmol) Jfl 30 3 4RYR 1 Y. L 4 J4LP- M 267 mg (1.96 mmo1)-t TJHF4 ml 1 WPM, C.tL{L 1-4 370 mng 30 mmo1) RflYPd 4 75 mg 065 mmol) -qS 1 4 2 N~ Jgk l AVPCAlA\ MgS0 4
LM
W 4L-A4,j XI-2 142 mg (19 Yo) Az4t 4L ^A 4 XI-2 1 H-NMR (400 MHz, DMSO-d 6 309C) 7. 81 (dld. J= 12. 7, 2. 0 Hz, 1 7. 71 J 1. 7 Hz, 1 7. 69 (dd, J 10. 3, 1. 7 Hz, 1 7. 54 (dd, J 1. 9 Hz, 1 7. 39 T 8. 3 Hz, 1 7. 15 J- 3. 7 Hz, 1H), 7. 12 J= 10. 5 Hz, 1 7. 09 J 12. 9 Hz, 1 7. 07 J3. 7 Hz, 1 3. 89 3 1. 66 4 H), 1. 31 6 1. 26 6 H) 0 t-!N'4 *XI-2 135 mg 35 mmo) =37 4 ml 2 N AKO th 1] 4UZ 1. 5 ml -Mk t!1f M.-l t 2 Pj. RIM V dU 2 N71 MHz, DMSO-d, 30-C) 7. 91 J= 12. 0 Hz, 2 H1), 7. 70 J1. 7 Hz, 1 H), 7. 55 (dd, J 8. 0, 2. 0 Hz, 1 7. 38 J= 8. 3 Hiz, 1 7. 28 J= 12. 0 WO 02/053523 WO 02/53523PCT/JP01111083 Hz, 2 7. 16 j 7Hz, 1 7. 08 J 7Hz, I1H), 1. 66 4 1. 32 6 1. 26 6 H) Anal. Calcd for C 25
H,
6 0, 1/4H 2 0 C (79. 23 H 05 Found C (79. 43 H 12 2- 4-7Z 1 4 t /tmJ/" -U 22 OtD I 0 4L-A4-J 176 0 C 'H-NMR (400 MHz, DMSO-d 6 30 0 C) 7. 80 J 12. 2 Hz, 2 7. 57 (d, J= 3. 9 Hz, 1 7. 51 J= 3. 9 Hz, 1 7. 42 (dd, J= 8. 3, 2. 2 Hz, 1 7. 37 J 8. 6 Hz, 1 7. 24 J= 12. 0 Hz, 1 H1), 1. 66 4 H), 1. 29 6 1. 25 6 H) Anal. Calcd f or C 2 1H 26 1S 1 C (76. 89 H 71 Found C (76. 68 H 84 ~J24 t/4K0i Tp250 B+ I AICI 3 Br 1) ii-BuLi I ZnCi2 ci 63% 2) Pd(PPh 3 4 1 1-4 XII-1 21% 0 0 OMe NaH~/OH 62% XII-2 -9-z 2. 92 g(15.9 nimol) *74b#]2-2 m t)K LTA- %AMSO 3Cm Z±A U 6 WO 02/053523 PCT/JP01111083 iti XI-1 2. 88 g (63 SfL-ij~'jXII-1 'H-NMR (400 MHz, CDCL 3 7.90 J 2.0 Hz, 1 7.73 1 7.67 1 7.59 J 8.6 Hz, 1 7.41 (dd, J 9.4, 2.0 Hz, 1 1.76 4 1.38 6 1.38 (s, 6 H) 4LIM't10XII-1 796 mg (2.51 mmol) i-THF 5 ml -78 9C t\ n-? 72I 16 M 5 olution in hexane) 2. 35 ml 77 nmol) tjaLN U ft. 0) Mf -z;Lrtt 4 L K! n (I1) 342 m g (2.51 mmol) BTHF4 ml I 4) 4{l x i 1n 2KUT 1 R t 6 t- V I 1-4 415 mg 67 mmol) .RtiOPd(PPhl),496mg 08 mmol) ITHF 7 ml Lgb: t U t 2 *rI 5J(-jAjII hNM t- 2 N A"t ~i a (iE -jv) C.vrq 4L XII-2 198 mg (21 4 7'c* 4L-At-tXII-2 'H-NMIR (400 MHz, DMSO-d., 300C) 8.02 1 7.94 (s, 1 7.90 1 7.89 J 9.3 Hz, 1 7.75 (dd, J 12.9, 2.2 Hz, 1 7. 49-7.63 2 7. 17 J 12. 7 Hz, 1 7.11 J 10. 7 Hz, 1 3.90 3 1.74 4 1.37 12 H), 40-~1 iXII-2 150 mg 40 mmol) n- '7 ml U, 2 N 7}z'Ltt A 3 m 1 11 P 7 0 'C T' Tf U It. 3 0 3 r -7 L- t- T U 2 N 7 0~ L t t, A L~ 6 A, 5(E 3 t- V, M- tS -it, 4, -4 IRi~j L 0) IM: 7j" LYNA A L UN t' L L t- t, W4 k.7 #A fr \7 MgSO 4 j L7bc Li, 4L-t Tp250 lt)tt 89 mg (62 ~i~4l O 4L= i Tp250 t~iV F (9=kr n -YL- L) &W 192 OC ;H-NMR (400 MHz, DMSO-d 6 30 0 C) 8.03 1 7.95 1 7.90 1 7.89 (d, J 9. 5 Hz, 1 7.78 J It. 9 Hz, 2 7.60 (dd, J 8. 3, 1. 7 Hz, 1 WO 02/053523 PCT/JP01111083 7.33 J 11.7 Hz, 2 1.74 4 1.37 12 H) Anal. Calcd for C 2 6HZ6O 2 C (83.76 H (7.31 Found C (83. 49 H (7.52 AJ 25 JL-r=6-Tp2600~5t OEt ryOEt K 2 C0 3 SQ-AOEt PPA OEt 81% 63% S XIII-I XIII-2 1) n-BuLi/ ZnC[ 2 OMe NaOH
OH
2) Pd(PPh 3 4 /L-4 quant. y XII1-3 Tp 26 0 6, 7, 8-5z 1 Kt I 5, 8, 8-7 1 A f/'-2-'yJ7s 550 mg 50 mmol) LeDMF 4 ml 9 L gE tj 9 'jY7 691 mg 00 mmol) 7"t -7 lt bT/V~L5 0. 45 ml (591 minol, 3.00 mmol) ;kaU-Cn' *J 40, 140 -C,4*4 ft .L~/5 0 3 R k 7.l~r/L L U, 4LfKb XIII-1 677 mg (81 t4 4c1. XIII-1 'H-NMR (400 MHz, CDCL,) 7. 32 J 2. 0 Hz, 1 7. 21 J 8. 3 Hz, 1 7. 15 (dd, J 8. 3, 2. 2 Hz, 1 4.B4 J 5.6 Hz, 1 3.66 J 7.1 Hz, 2 3.54 J 7. 1 Hz, 2 3. 10 J 5. 6 Hz, 2 H1), 1. 66 4 1. 26 6 1. 6 1.19 J 7.1 Hz, 6 H), L-t1S XIII-2 673 mg 00 mmol) L bWc.>' 2. 5 ml -'Mr PPA g 90 0 CTN41LU-/.O 1 *rmj j 7PhP- ,z5L lC"tI W4 U, cj( A\MgSO 4 Z U- 7 WO 02/053523 PCT/JP01111083 Y ,/L3 5 7 n- 1 1 0) Tr$ L, 4L' XIII-2 309 mg (63 l) jo4f ~L-617 XII1-2 1 1-NMR (400 MHz, CDCL) 7.82 1 7.77 1 7.31 J 5.4 Hz, 1 7.22 J 4.9 Hz, 1 1.75 4 1.36 6 1.35 6 Hl) X't= JIII-2 192 mg 79 mmo1) THF 2 mli L -78 'C ir- C n-BuLi 1. 6 M k- 4VO 0. 74 ml 19 mmcl) ~ib~ 30 tL O, OD 4'{lM M 108 mg 79 mmo1) l- THF 2 ml I J ft V L il Ut'k 1 Ri-rMN, i- 11-2 149 mg 52 mmol) XZY Pd (PPh 3 4 30 mg 026 mmol) THF4ml U It t VD (LIN -M RT)JR1 t 3 RHO 7tu,-. WO 34 mg (15 C 8i' 4L- XIII-3 'H-NMR (400 MHz, CDCL) 7. 75 1 H), 7.72 1 7.71 (dd, J 12.7, 2.0 Hz, 111), 7.43 1 7.43 (dd, J 10.5, 2.0 Hz, 1 7.30 J 12.7 Hz, 1 6.82 J 10.7 Hz, 1 3.99 3 1.75 4 1.36 12 H) 0 {L'tf~j XIII-3 32 mg 085 mml) m 2 ml U, 2 N 7J1Y"fKY 9 1' A I m 1K)- P Z ME It J* At 3 3 J 2 N A MR K, L7', 'fi R Tp260 O)RttY t 32 mg (quant) V ft. 4L-h-AOj Tp260 (Wft J4E./-IV iJli~\ 172 0 C 'H-NMR (400 MHz, DMSO-d 6 30 C) 7. 91 (s, 1 7.81 J 12.0 Hz, 2 7.78 1 7.74 I 7.27 J 12.0 Hz, 2 1.69 4 1.32 12 H) Anal. Calcd for C 23
H
24 0,S, C (75. 79 H 64 Found C (75. 49 H 69 WO 02/053523 PCT/JP01111083 ~1 1: 4~~14L~~J~L W0 I4 3JZI X 10" M 0) H1X630 *750I-,1o 61-76440 4 tt~~m! 1i IJ~h~ 1-60 O-C Wft**\ 3a): L. 1 M10 f6l 0 N 0 1U' WO 02/053523 WO 02/53523PCT/JP01111083 1 x 10-7 M HX630 tii-irz Tp 10 Tp2O Tp22 Tp 50 Tp8O Tp82 Tp84 Tp88 Tp93 TpA14 Tp 141 Tp 145 Tp146 Tp 149 Tp 150 Tp155 -8 0. 6 6. 8 2. 1 2. 8 1. 3 1. 3 1. 6 0. 8 7 0. 5 0. 7 0. 9 0. 7 0. 6 0. 5 65 2. 2 73 3. 6 1.4 1. 5 2. 7 -7 0. 5 2. 9 1.8 2.4 1. 5 0. 9 2. 8 1. 3 26 1. 2 5 1.2 0. 9 0. 8 0. 5 73 3. 3 76 2. 2 4 5.4 24 -6 13 3. 3 2. 7 18 1. 2 2. 3 5. 1 2. 1 21 1.4 26 46 67 9 0. 3 14 6.4 70 69 40 60 62. 5 2. 2 82 1. 9 15 2. 6 1. 5 3. 6 0. 8 89 4. 1 82 66 3. 5 9 68 -7 1.2 2. 9 3. 7 3. 3 2. 3 2. 5 21. 2 85 7 89 14 2. 1 0. 8 0. 5 93 7 75 91 85 80 89 -6 5.6 2.4 78 2 37. 8 79 42 62 43 1.7 66 84 77 83 78- Tp160 18. 5 34. 4 32 Tpl7O Tp175 TP 180 Tpl9O Tp200 Tp2 10 Tp260 0. 8 1. 2 0. 5 32 14 6 66 20 81 84 0. 5 2.3 3 2 33 2. 7 2.6 33 77 90 77 95 64 91 91 91 84 79 91 83 67 J7XtU F ",Z7 MR
Claims (7)
1. A medicament comprising the compound represented by the following general Z formula or a salt thereof ON R 1 cI0 00 R 4 cO IN ci (I) C] 5 wherein R 2 R 3 and R 4 independently represent hydrogen atom, a alkyl 0 group, said alkyl group may be substituted, or a alkoxyl group, and when R 2 and R 3 are adjacent to each other, they may combine together with carbon atoms of the phenyl group to which R 2 and R 3 bind to form a 5- or 6-membered ring, said ring may have one or more C,-C 4 alkyl groups or one condensed benzene ring which may. have one or more substituents on the ring; the ring represented by Ar represents an aryl ring; X represents a single bond, -CON(Rs)-, (wherein R 5 represents hydrogen atom or a alkyl group), wherein n represents an integer of 1 to 3, and R 6 represents hydrogen atom or a alkyl group, -N(R T CON(R 8 R 7 and R 8 represent hydrogen atom or a C,-C alkyl group, -SO 2 N(R 9 R 9 represents hydrogen atom or a alkyl group, -N(R 1 0 R' 0 represents hydrogen atom, a alkyl group, or a C,-C acyl group, a Ci-C, alkylene group, said alkylene group may contain one or more unsaturated bonds or a cyclic structure, an aryldiyl group; Y represents hydrogen atom, -OR 11 R 1 represents hydrogen atom, a Cl-C, alkyl group, or a C,-C 6 acyl group, -NHR' 2 R' 2 represents hydrogen atom, a alkyl group, a acyl group, or amino group, or a halogen atom.
2. The medicament of claim 1 wherein R 4 is hydrogen atom or a alkyl group, Y is hydrogen atom, hydroxyl group, a C,-Ce alkoxyl group, hydrazino group, or a halogen atom.
3. A method for treating leukemia, comprising administering a pharmaceutical composition of the medicament according to claim 2 in a therapeutically effective amount. I: COMS ID No: ARCS-170595 Received by IP Australia: Time 16:33 Date 2007-11-29 29/11/207 14:54 COLLISON CO FDELFIDE 0262837999 N0.899 o009
4. A pharmaceutical composition comprising the compound or a physiologically acceptable salt thereof according to claim 2. A method for treating leukemia, comprising administering a pharmaceutical composition according to claim 5 in a therapeutically effective amount.
6. The medicament of claim 1 wherein the compound or salt thereof according to claim 1, is a compound or salt thereof of the following formula: wherein R 1 and R 5 are hydrogen.
8. A pharmaceutical composition comprising the compound or a physiologically acceptable salt thereof according to claim 7.
9. A method for treating leukemia, comprising administering a pharmaceutical composition according to claim 7 in a therapeutically effective amount. COMS ID No: ARCS-170595 Received by IP Australia: Time 16:33 Date 2007-11-29
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000394338 | 2000-12-26 | ||
JP2000-394338 | 2000-12-26 | ||
PCT/JP2001/011083 WO2002053523A1 (en) | 2000-12-26 | 2001-12-18 | Tropolone derivative |
Publications (3)
Publication Number | Publication Date |
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AU2002222682A1 AU2002222682A1 (en) | 2003-01-23 |
AU2002222682B2 AU2002222682B2 (en) | 2007-12-13 |
AU2002222682B8 true AU2002222682B8 (en) | 2008-05-29 |
Family
ID=18859983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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AU2002222682A Ceased AU2002222682B8 (en) | 2000-12-26 | 2001-12-18 | Tropolone Derivatives |
Country Status (8)
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US (1) | US7259187B2 (en) |
EP (1) | EP1357104A4 (en) |
JP (1) | JPWO2002053523A1 (en) |
KR (1) | KR20030077558A (en) |
CN (1) | CN1247511C (en) |
AU (1) | AU2002222682B8 (en) |
CA (1) | CA2432409A1 (en) |
WO (1) | WO2002053523A1 (en) |
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EP1733722A4 (en) * | 2004-03-10 | 2010-07-14 | Res Found Itsuu Lab | Memory fixation accelerator |
WO2007037188A1 (en) * | 2005-09-27 | 2007-04-05 | Sapporo Medical University | Pharmaceutical for prevention and treatment of ophthalmic disease induced by increase in vasopermeability |
US7427316B2 (en) * | 2005-12-30 | 2008-09-23 | E.I. Du Pont De Nemours And Company | Tropolone complexes as wood preservatives |
US7540906B2 (en) * | 2005-12-30 | 2009-06-02 | E.I. Du Pont De Nemours & Company | Metal salts of hydrolyzed olefin/maleic anhydride copolymers and their use as wood preservatives |
US7462227B2 (en) * | 2005-12-30 | 2008-12-09 | E.I. Du Pont De Nemours And Company | Ibuprofen complexes as wood preservatives |
US7497901B2 (en) * | 2005-12-30 | 2009-03-03 | E. I. Dupont De Nemours And Company | Tungstate and molybate wood preservatives |
EP2513057B1 (en) * | 2009-12-14 | 2013-09-04 | Merck Patent GmbH | Sphingosine kinase inhibitors |
JP2013514287A (en) * | 2009-12-17 | 2013-04-25 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | Inhibitors of sphingosine kinase |
WO2013038931A1 (en) * | 2011-09-12 | 2013-03-21 | 壽製薬株式会社 | Method of producing 2-oxo-2h-cyclohepta[b]furan analogue |
JP7503310B2 (en) * | 2018-04-13 | 2024-06-20 | ザ ボード オブ トラスティーズ オブ ザ ユニヴァーシティ オブ イリノイ | Hinokitiol analogues, their preparation methods and pharmaceutical compositions |
CN109776357A (en) * | 2018-08-29 | 2019-05-21 | 湖北工业大学 | A kind of micromolecular inhibitor containing tropolone and the application in inhibition ornithine decarboxylase (ODC) |
EP4045477A4 (en) * | 2019-10-16 | 2024-09-25 | Kinesid Therapeutics Inc | Tropolone derivatives and tautomers thereof for iron regulation in animals |
WO2021076945A1 (en) * | 2019-10-16 | 2021-04-22 | Ambys Medicines, Inc. | Tropolone derivatives and tautomers thereof for iron regulation in animals |
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JPS4314705Y1 (en) | 1965-09-09 | 1968-06-20 | ||
FR2080201A6 (en) | 1970-02-26 | 1971-11-12 | Wendel Sidelor | |
JPS6176440A (en) | 1984-09-19 | 1986-04-18 | Koichi Shiyudo | Benzoic acid derivative |
JPS6122047A (en) | 1984-07-07 | 1986-01-30 | Koichi Shiyudo | Benzoic acid derivative |
JPS61215341A (en) * | 1985-03-20 | 1986-09-25 | Masatoshi Yamato | Production of tropolone derivative and use as antitumor agent |
US5235076A (en) | 1991-05-28 | 1993-08-10 | University Of Hawaii | Azulenic retinoid compounds, compositions and methods |
WO1995004036A1 (en) | 1993-01-11 | 1995-02-09 | Ligand Pharmaceuticals Inc. | Compounds having selective activity for retinoid x receptors, and means for modulation of processes mediated by retinoid x receptors |
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2001
- 2001-12-18 AU AU2002222682A patent/AU2002222682B8/en not_active Ceased
- 2001-12-18 CN CNB018227716A patent/CN1247511C/en not_active Expired - Fee Related
- 2001-12-18 CA CA002432409A patent/CA2432409A1/en not_active Abandoned
- 2001-12-18 WO PCT/JP2001/011083 patent/WO2002053523A1/en active Application Filing
- 2001-12-18 US US10/450,836 patent/US7259187B2/en not_active Expired - Fee Related
- 2001-12-18 KR KR10-2003-7008558A patent/KR20030077558A/en active IP Right Grant
- 2001-12-18 JP JP2002554642A patent/JPWO2002053523A1/en not_active Ceased
- 2001-12-18 EP EP01272512A patent/EP1357104A4/en not_active Withdrawn
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EP1357104A1 (en) | 2003-10-29 |
WO2002053523A1 (en) | 2002-07-11 |
US7259187B2 (en) | 2007-08-21 |
CN1247511C (en) | 2006-03-29 |
AU2002222682B2 (en) | 2007-12-13 |
US20040082550A1 (en) | 2004-04-29 |
CA2432409A1 (en) | 2002-07-11 |
EP1357104A4 (en) | 2004-07-28 |
KR20030077558A (en) | 2003-10-01 |
CN1491197A (en) | 2004-04-21 |
JPWO2002053523A1 (en) | 2004-04-30 |
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